New gene fragment, novel transgenic zebrafish and methods for producing transgenic zebrafish

a technology of transgenic zebrafish and gene fragment, which is applied in the field of new gene fragment, novel transgenic zebrafish and methods for producing transgenic zebrafish, can solve the problems of unfavorable human development, inability to easily deduce, and inability to develop gene-targeting protocols in the ra

Inactive Publication Date: 2009-05-21
TAIKONG +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although the transgenic green and red fluorescence zebrafishs have been described, method and condition of generating other transgenic fish with other gene fragment (such as red fluorescent protein expressed by β-actin promoter) is different and cannot be easily deduced from the prior art because of the different strategies of genetic construction, gene expression, gene inheritance and uncertainties of the transgenic technique.
The gene targeting is well established in the mouse; however, gene-targeting protocols have not been developed in the rat despite the establishment more than 16 years ago of the first transgenic rats by pronuclear injection (F Kent Hamra et al.
Therefore, the results of similar gene fragment expressed in different species are unpredictable and worth studying.

Method used

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  • New gene fragment, novel transgenic zebrafish and methods for producing transgenic zebrafish
  • New gene fragment, novel transgenic zebrafish and methods for producing transgenic zebrafish
  • New gene fragment, novel transgenic zebrafish and methods for producing transgenic zebrafish

Examples

Experimental program
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Effect test

example 1

Generation of the Plasmid pZβ-DsRed2-1-ITR

[0046]Commercially available plasmid construct, pDsRed2-1 (Clontech) was used to generate the expression vector.

[0047]The DsRed 2-1 fragment was from plasmid pDsRed2-1. The CMV promoter and two adeno-associated virus inverted terminal repeats (ITR) were ligated to the DsRed2-1 fragment as depicted in FIG. 1 to produce plasmid construct pDsRed2-1-ITR. The plasmid construct pDsRed2-1-ITR has shown higher expression stability.

Generating the Novel Plasmid Construct: pZβ-DsRed2-1-ITR

[0048]As illustrated in FIG. 1, the zebrafish β-actin gene promoter was obtained by digesting plasmid construct pOBA-109 with restriction enzymes BamHI and SalI. BamHI was used first, ends were filled in, and a subsequent digestion with SalI provided a 4775 bp fragment.

[0049]As illustrated in FIG. 1, the CMV promoter was cut out by digesting the construct pDsRed2-1-ITR with restriction enzymes BamHI and SalI. Digestion with BamHI and SalI provided a 4240 bp fragment. ...

example 2

Preparation of Microinjected DNA

[0052]All DNA plasmids were prepared via ultra-centrifugation with cesium chloride and ethidium bromide gradient (Radloff et al., 1967 Proc Natl Acad Sci USA 57:1514-1521). All DNA fragments used for microinjection were eluted from agarose gel following electrophoresis.

example 3

Cytoplasmic Microinjection

[0053]Fish were maintained under artificial conditions of 14 h light and 10 h darkness at 26° C. and maintained on a diet of Tetramin (Tetra, Germany). Before the incubator entered the dark cycle, fish were collected and separated by separation net. On the next morning after the light cycle has begun, fish eggs were collected every 15-20 minutes.

[0054]Eggs were collected within 30 minutes of fertilization and attaching filaments removed. The linearized construct was quantified and dissolved in 5×PBS with phenol red at the desired concentration. DNA was picked up by micro-capillary of zebrafish microinjector (Drummond) wherein the injection needle width of the micro-capillary was approximately 10 μm. As micro-needle enters the cell cytoplasm, the DNA injected was approximated 2-3 nl. In each microinjection session, 30-40 eggs were injected; 250-300 eggs were injected in each experiment. Injected eggs were incubated at 26° C. in distilled water.

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Abstract

The present invention provides a method for producing systemic red fluorescent zebrafish. The present invention also provides a new gene fragment and a systemic red fluorescent zebrafish.

Description

FIELD OF THE INVENTION[0001]The present invention relates to a method for producing novel transgenic zebrafish.[0002]The present invention also relates to a new gene fragment and novel transgenic zebrafish.BACKGROUND OF THE INVENTION[0003]Transgenic ornamental fish is one sector of the fishery business and belong to entertainment industry with global business. For example, transgenic fish expressing green fluorescence by introduction of a GFP gene fused with a fish-specific gene promoter into fertilized eggs, has been generated using zebrafish (Hamada, K. et al., Mol. Marine Biol. Biotech., 1998. 7, 173-180).[0004]Hsiao et al. disclosed a DNA construct flanked at both ends by inverted terminal repeats (ITRs) to increase the efficient expression of transgenic genes in zebrafish. A uniform transgene expression was achieved in the F0 and the following two generations (Hsiao et al., Developmental Dynamics 2001. 220: 323-336). US 2004 / 0117866 A1 also disclosed a similar gene fragment for...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A01K67/027C07H21/04C12N15/00
CPCA01K67/0275A01K2217/052A01K2227/40C12N15/8509C07K14/43595C07K14/4716A01K2267/0393
Inventor TSAI, HUAI-JEN
Owner TAIKONG
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